# Axiom, Inc.

- Location (FDA's records): Mchenry, IL
- FDA decisions: 4 (1984–1989): 4 510(k) clearances
- Product codes: CDT (1), KNK (1), GBS (1), CHH (1)
- Predicates its devices cite: 0 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Recent decisions
- K883887: Axiom Atraum Wound Drains (Feb 17, 1989)
- K842443: Axiom Stable II Triglycerides Test (Sep 13, 1984)
- K842442: Axiom Stable II Uric Acid Test (Aug 16, 1984)
- K842441: Axiom Stable II Cholesterol Test (Jul 25, 1984)

Source page: https://510kreport.com/company/axiom